Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs75501914 4 3448054 intron variant G/A snv 7.9E-02 5.6E-02 2